Porous manganese oxide nanoparticles and method for preparing the same

ABSTRACT

The disclosure relates to porous manganese oxide nanoparticles which include flocculated primary nanoparticles, with air pores formed between the primary nanoparticles. Unlike in the prior art, the porous manganese oxide nanoparticles of the disclosure have 6 nm or less MnO 2  primary nanoparticles and Mn 3 O 4  primary nanoparticles uniformly mixed and flocculated, exhibiting a 16 times higher specific surface area as compared with the conventional manganese oxide particles and superior storage characteristics and stability.

CROSS-REFERENCE TO RELATED APPLICATION(S)

This application is based on and claims priority under 35 U.S.C. 119 to Korean Patent Application No. 10-2019-0058532, filed on May 20, 2019, in the Korean Intellectual Property Office, the disclosure of which is herein incorporated by reference in its entirety.

TECHNICAL FIELD

The present disclosure relates to porous manganese oxide nanoparticles and a method for preparing the same, and more specifically, to porous manganese oxide nanoparticles, into which Mn₃O₄ primary nanoparticles and MnO₂ primary nanoparticles have been mixed and flocculated, and a method for preparing the same.

DISCUSSION OF RELATED ART

Manganese oxide is used as negative electrode for lithium secondary batteries. Generally, the negative electrode material requires a smaller particle size and larger specific surface area to enhance charging/discharging properties in the high current density of lithium secondary battery. Manganese oxide is used as a material for preparing lithium manganate which is used as positive active material for secondary batteries. An effective method for preparing small particle lithium manganate is to use small size manganese oxide as raw material. Manganese oxide powder may be adopted for various purposes, e.g., super capacitor electrodes, semiconductor material, sensors, pigment, catalysts, or water treatment. Thus, the smaller the particle size is, the better properties may be achieved for cobalt oxide powder. In this sense, it is critical to prepare a nanosized manganese oxide powder.

Top-down processed, which are based on milling, and bottom-up processes, which are chemical processes, have conventionally been employed to prepare nanosized metal oxide particles.

Korean Patent No. 10-1184730 discloses a top-down process for preparing a nano powder by milling cerium oxide powder slurry twice, with the RPM controlled. Korean Patent Application Publication No. 10-2009-0007451 discloses a method for preparing a cerium oxide nano powder containing cerium oxide particles with a particle size of 100 nm or more. This prior art regards a bottom-up process for preparing cerium oxide nana particles by forming cerium hydroxide sediment by mixing a cerium salt and an alkali solution and then performing hydrothermal synthesis.

However, such conventional methods fail to prepare manganese oxide particles with a particle size of 10 nm or less.

Further, upon using manganese oxide as electrode material for lithium secondary batteries, it may be effective to mix MnO₂ which has superior lithium ion storage characteristics, and Mn₃O₄ which shows high stability.

The conventional methods to prepare a mixed powder of Mn₃O₄ and MnO₂ are to individually prepare a Mn₃O₄ powder and an MnO₂ powder and then mix them up. Thus, the blend uniformity issue ensues.

SUMMARY

According to an embodiment, there are provided porous manganese oxide nanoparticles which have a 16 times higher specific surface area in unit volume than the conventional manganese oxide particles and, when applied to batteries, exhibit superior storage characteristics and stability because they have 6 nm or less MnO₂ nanoparticles and Mn₃O6 ₄ nanoparticles mixed and flocculated.

According to an embodiment, there is provided a method for preparing porous manganese oxide nanoparticles in the form of 6 nm or less MnO₂ primary nanoparticles and Mn₃O₄ primary nanoparticles mixed and flocculated by separating Mn clusters by injecting positive ions into the Mn₃O₄ lattices.

According to an embodiment, there are provided porous manganese oxide nanoparticles configured in a form of flocculated primary nanoparticles represented as in chemical formula 1 and primary nanoparticles represented as in chemical formula 2, wherein air pores are formed between the primary nanoparticles, wherein

Mn₃O_(4-x)   [Chemical Formula 1]

where 0≤×≤0.4.

MnO_(2-y)   [Chemical Formula 2]

where 0≤33 ≤0.2.

In the porous manganese oxide nanoparticles, the volume ratio of the primary nanoparticles represented as in chemical formula 1 to the primary nanoparticles represented as in chemical formula 2 may range from 10% to 90%.

In the porous manganese oxide nanoparticles, the primary nanoparticles represented as in chemical formula 1 and the primary nanoparticles represented as in chemical formula 2 may be evenly or uniformly flocculated.

The size of the primary nanoparticles represented as in chemical formula 1 or 2 may be 0.3 nm to 6 nm.

The porosity of the porous manganese oxide nanoparticles may range from 10% to 40%.

The size of the air pore may range from 0.4 nm to 6 nm.

The BET specific surface area of the porous manganese oxide nanoparticles may range from 60 m²/g to 120 m²/g.

According to an embodiment, there may be provided porous manganese oxide nanoparticles prepared by forming first nanoparticles represented as in chemical formula 1 in such a method as to separate Mn clusters by injecting positive ions into lattices of Mn₃O₄ particles and forming second nanoparticles represented as in chemical formula 2 by partially reducing the first nanoparticles, wherein

Mn₃O_(4-x)   [Chemical formula 1]

where 0≤×≤0.4.

MnO_(2-y)   [Chemical formula 2]

where 0≤×≤0.2.

In the porous manganese oxide nanoparticles, the volume ratio of the first nanoparticles represented as in chemical formula 1 to the second nanoparticles represented as in chemical formula 2 may range from 10% to 90%.

In the porous manganese oxide nanoparticles, the first nanoparticles represented as in chemical formula 1 and the second nanoparticles represented as in chemical formula 2 may be evenly or uniformly flocculated.

The positive ions may be positive ions of an alkaline metal or an alkaline earth metal.

The positive ions may be injected using a constant current or constant voltage method.

According to an embodiment, a method for preparing porous manganese oxide nanoparticles comprises placing an Mn₃O₄ thin film layer and an ion generation layer on two opposite surfaces of a separation plate and applying a voltage to the Mn₃O₄ thin film layer and the ion generation layer. The ion generation layer includes an alkaline metal, an alkaline earth metal, an alkaline metal-containing alloy, or an alkaline earth metal-containing alloy.

The Mn₃O₄ thin film layer may be formed by casting slurry on a metal sheet and drying the slurry-cast metal sheet. The slurry may be formed by mixing an Mn₃O₄ powder, a binder, and an organic solvent.

The ion generation layer may include an alkaline metal, an alkaline earth metal, an alkaline metal-containing alloy, or an alkaline earth metal-containing alloy.

The separation plate may be formed by wetting a porous polymer plate with an electrolyte.

Unlike in the prior art, the porous manganese oxide nanoparticles of the disclosure have 6 nm or less MnO₂ primary nanoparticles and Mn₃O₄ primary nanoparticles uniformly mixed and flocculated, exhibiting a 16 times higher specific surface area as compared with the conventional manganese oxide particles and superior storage characteristics and stability.

According to an embodiment, the method may prepare porous manganese oxide nanoparticles in the form of 6 nm or less MnO₂ primary nanoparticles and Mn₃O₄ primary nanoparticles mixed and flocculated by separating Mn clusters by injecting positive ions into the Mn₃O₄ lattices.

BRIEF DESCRIPTION OF THE DRAWINGS

A more complete appreciation of the present disclosure and many of the attendant aspects thereof will be readily obtained as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings, wherein:

FIG. 1 is a view schematically illustrating a process for preparing porous manganese oxide nanoparticles according to an embodiment;

FIG. 2 is a galvanostatic cycling with potential limitation (GCPL) of porous manganese oxide nanoparticles preparing device according to an embodiment;

FIG. 3 is a view illustrating the results of TEM measurement on a comparative example;

FIG. 4 is a view illustrating the results of high-resolution TEM measurement on a comparative example; and

FIG. 5 is a view illustrating the results of TEM measurement on an embodiment.

DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS

Hereinafter, exemplary embodiments of the inventive concept will be described in detail with reference to the accompanying drawings. The inventive concept, however, may be modified in various different ways, and should not be construed as limited to the embodiments set forth herein. Like reference denotations may be used to refer to the same or similar elements throughout the specification and the drawings.

When determined to make the subject matter of the present disclosure unclear, the detailed description of the known art or functions may be skipped.

The terms as used herein are provided merely to describe some embodiments thereof, but not to limit the present disclosure. As used herein, the singular forms “a,” “an,” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “comprise” and/or “have,” when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof.

Hereinafter, embodiments of the present disclosure are described in detail. However, the scope of the disclosure is not limited to the embodiments disclosed herein but is defined by the appended claims.

The disclosure relates to porous manganese oxide nanoparticles which include flocculated primary nanoparticles, with air pores formed between the primary nanoparticles.

The primary nanoparticles may be represented as in chemical formula 1 or 2 below.

Mn₃O_(4-x)   [Chemical formula 1]

where 0≤×≤0.4.

MnO_(2-y)   [Chemical formula 2]

where 0≤×≤0.2.

The primary nanoparticles mean particles that result as Mn₃O₄ particles have air pores built up therebetween and their bonds are broken. As positive ions are injected into the lattices, the primary nanoparticles are reduced as in chemical formula 1 or 2. Flocculation may be the gathering of primary nanoparticles that are formed as air pores build up inside the secondary particles (Mn₃O₄ particles), which are of the parent phase, the interparticle bonds are broken. The gaps between the primary nanoparticles may be the air pores.

The volume ratio of the primary nanoparticles represented as in chemical formula 1 to the primary nanoparticles represented as in chemical formula 2 may range from 10% to 90%.

Preferably, the primary nanoparticles represented as in chemical formula 1 and the primary nanoparticles represented as in chemical formula 2 may be evenly or uniformly flocculated.

The primary nanoparticles represented as in chemical formula 1 may exhibit excellent stability when applied to batteries, and the primary nanoparticles represented as in chemical formula 2 may show superior storage characteristics. Thus, as the primary nanoparticles represented as in chemical formula 1 and the primary nanoparticles represented as in chemical formula 2 are mixed more uniformly, better battery characteristics may be obtained. Unlike the conventional mixed powder of Mn₃O₄ and MnO₂, which is obtained by simply mixing an Mn₃O₄ powder and an MnO₂ powder, the porous manganese oxide nanoparticles, according to an embodiment, may be formed as the primary nanoparticles are mixed and flocculated, showing superior uniformity.

The size of the primary nanoparticles represented as in chemical formula 1 or 2 may be 0.3 nm to 6 nm.

The amorphous primary nanoparticles with a size less than 0.3 nm are nearly impossible to prepare, and although possible, they may be hard to use commercially. If the size of the primary nanoparticles exceeds 6 nm, no or little confinement effect of a specific size may be achieved and, thus, the increase in reaction efficiency may be limited.

The porosity of the porous manganese oxide nanoparticles may range from 10% to 40%. If the porosity is less than 10%, the passage of substrate molecules may be restricted and, thus, reactivity may be lowered. If the porosity exceeds 40%, the passage of the molecules is smooth, but a narrow confinement effect of a specific size may not arise and an increase in reaction efficiency may be limited.

The size of the air pore may range from 0.4 nm to 6 nm. If the size of the air pore is less than 0.4 nm, the passage of substrate molecules may be restricted and, thus, reactivity may be lowered. If the size of the air pore exceeds 6 nm, the passage of the molecules is smooth, but a narrow confinement effect of a specific size may not arise and an increase in reaction efficiency may be limited.

The BET specific surface area of the porous manganese oxide nanoparticles may range from 60 m²/g to 120 m²/g. This is about 400 times larger than the conventional manganese oxide particles. If the BET specific surface area is less than 60 m²/g, the reactivity is lowered and, if the BET specific surface area is more than 120 m²/g, no narrow confinement effect of a specific size results, restricting an increase in reaction efficiency.

According to an embodiment, the porous manganese oxide nanoparticles may be prepared by forming the first nanoparticles represented as in chemical formula 1 in such a method as to separate the Mn clusters by injecting positive ions into the lattices of Mn₃O₄ particles and forming the second nanoparticles represented as in chemical formula 2 by partially reducing the first nanoparticles.

Specifically, if positive ions are injected into the lattices of Mn₃O₄ particles, lattice distortion occurs. Defects in lattice, vacancy defects, or grain boundaries are given depending on the amount of positive ions injected, and the shape and concentration are precisely controlled to form lattices with a new property. The bonds in the lattices may be broken by worsening the lattice distortion and, thus, ultrafine particles may be formed.

In the porous manganese oxide nanoparticles according to an embodiment, primary nanoparticles (i.e., the first nanoparticles) represented as in chemical formula 1 are formed by breaking the intralattice bonds in such a manner as to worsen lattice distortion and, at this time, the primary nanoparticles (i.e., the first nanoparticles) represented as in chemical formula 1 are reduced into primary nanoparticles (i.e., the second nanoparticles) represented as in chemical formula 2 by the positive ions simultaneously injected. Thus, the first nanoparticles represented as in chemical formula 1 and the second nanoparticles represented as in chemical formula 2 may be uniformly mixed and flocculated.

FIG. 1 schematically illustrates the above description. FIG. 1 illustrates a process in which as injection of positive ions worsens lattice distortion, Mn₃O₄ particles form air pores, and the first and second nanoparticles are mixed and flocculated into the porous manganese oxide nanoparticles.

The positive ions may be those of an alkaline metal or alkaline earth metal. For example, the positive ions may be those of lithium (Li), sodium (Na), potassium (K), magnesium (Mg), or calcium (Ca).

The positive ions may be injected by a constant current or constant voltage method.

Now described is a method for preparing porous manganese oxide nanoparticles according to an embodiment. However, embodiments of the disclosure are not limited thereto.

First, a Mn₃O₄ thin film layer and an ion generation layer are placed on both sides of a separation plate (step a).

Specifically, a Mn₃O₄ thin film layer is formed on a metal sheet, and then, the metal sheet is placed on a cathode electrode.

The Mn₃O₄ thin film layer may be formed by coating the metal sheet with, e.g., mixed slurry of Mn₃O₄ powder, a binder, and an organic solvent. The binder may include polyvinylidene fluoride (PVDF), Nafion, poly(acrylic acid) (PAA), carboxymethyl cellulose (CMC), styrene-butadiene rubber (SBR), polytetrafluoroethylene (PTFE), or poly(ethylene oxide).

The organic solvent may include N-Methyl-2-Pyrrolidone (NMP), ethanol, tetrahydrofuran (THF), benzene, KOH/MeOH, MeOH, toluene, CH₂Cl₂, hexane, dimethylformamide (DMF), di-isopropyl ether, diethyl ether, dioxane, dimethylacetamide (DMA), dimethyl sulfoxide (DMSO), or chlorobenzene.

The slurry may further include a conducting agent, such as super-p, Ketjenblack, acetylene black, sfg6, or CNT.

The weight ratio of the Mn₃O₄ powder to the binder in the slurry may be 90:10 to 99:1.

The weight ratio of the mixture of the Mn₃O₄ powder and the binder to the organic solvent may be 10 mg to 0.01 mL through 1 mL.

The weight ratio of the conducting agent to the slurry may be 0.1 mg through 0.5 mg to 10 mg.

The metal sheet may include a copper, aluminum, silver, or stainless steel sheet. As the metal sheet, any metal sheet with good conductivity may be used. A metal sheet with a reduction potential higher than about 0.0 V vs. RHE may be electrochemically preferable.

The thickness of the metal sheet may range from 10μm to 100μm.

The thickness of the Mn₃O₄ thin film layer may range from 10μm to 400μm.

The cathode electrode may include stainless steel, aluminum, titanium, copper, nickel, or an alloy thereof. Other various metals or alloys with oxide film passivity may be adopted for the metal sheet.

The thickness of the cathode electrode may range from 10μm to 1,000μm.

Next, an ion generation layer is formed on an anode electrode.

The ion generation layer may include an alkaline metal, an alkaline earth metal, an alkaline metal-containing alloy, or an alkaline earth metal-containing alloy, preferably lithium (Li), sodium (Na), potassium (K), magnesium (Mg), or calcium (Ca). The ion generation layer may be in the form of a metal sheet.

The thickness of the ion generation layer may range from 10μm to 1,000μm.

The anode electrode may include stainless steel, aluminum, titanium, copper, nickel, or an alloy thereof. Other various metals or alloys with oxide film passivity may be adopted for the metal sheet.

The thickness of the anode electrode may range from 10μm to 1,000μm.

The anode electrode and the cathode electrode are connected to terminals to which voltage is applied from the outside.

Then, the Mn₃O₄ thin film layer and the ion generation layer are placed on both sides of a separation plate.

The separation plate may be formed by wetting a porous polymer plate with an electrolyte.

The porous polymer plate may include, e.g., polypropylene (PP), polyethylene (PE), polytetrafluoroethylene (PTFE), alumina-coated polypropylene, cellulose, or polypropylene-polyethylene-polypropylene plate.

The thickness of the porous polymer plate may range from 10μm to 1,000μm.

The electrolyte may contain metal ions which are included in the ion generation layer.

Specifically, the electrolyte may include MPF6 (where M is the alkaline and alkaline earth metal ion)—dissolved EC, DEC, DMC, or other organic solvent solution or aqueous solution.

If the thickness of each layer is less than the lower limit, the layer may be easily torn and, if exceeding the upper limit, the layers may be difficult to join together due to an increase in the overall thickness.

Thereafter, a voltage is applied to the Mn304 thin film layer and the ion generation layer (step b).

If a voltage is applied to the Mn₃O₄ thin film layer and the ion generation layer, the potential difference causes oxidation, allowing alkaline metal or alkaline earth metal ions to build up on the ion generation layer. The alkaline metal or alkaline earth metal ions are dissolved in the electrolyte and pass through the separation plate to the Mn₃O₄ thin film layer. The separation plate, although electrically insulated, may allow ions to pass through. The alkaline metal or alkaline earth metal ion generated from the ion generation layer trigger reduction on the Mn3O₄ thin film layer, allowing the ions to be injected into the lattices. The injected ions may cause lattice distortion and, depending on the degree of distortion, intralattice defects may occur.

The degree of distortion may be adjusted depending on the degree of ion injection (voltage and time). As the voltage initially applied reduces, more ions may be injected into the Mn3O₄ thin film layer, increasing lattice distortion. The defects may include vacancies, oxygen vacancies, or boundaries. If the lattice bonds are broken by worsening the lattice distortion, ultra-fine particles (the first nanoparticles) may be generated and, at this time, some of the first nanoparticles may be reduced into the second nanoparticles. If the voltage is further lowered, the ions may be alloyed with the Mn metal, resulting in the formation of a manganese alloy. Thus, a caution needs to be taken. Such a proper amount of ions as to break the lattice bonds needs to be injected. Injection of less ions may cause defects but fail to break the bonds, and injection of more ions may result in the formation of a manganese alloy.

It is preferable to place the metal sheet on the Mn3O₄ thin film layer. By its conductivity, the metal sheet may transfer electrons to the Mn₃O₄ thin film layer. As such, because the metal sheet is stable upon injecting alkaline metal or alkaline earth metal ions into the Mn3O₄ thin film layer by applying voltage, application of the metal sheet is preferable.

To separate the porous manganese oxide nanoparticles in the form of flocculated primary nanoparticles represented as in chemical formula 1 or 2, the Mn₃O₄ thin film layer, the ion generation layer, and the separation plate are disassembled to separate the Mn₃O₄ thin film layer off, and the Mn₃O₄ thin film layer is washed with an organic solvent.

The organic solvent washes the electrolyte off the Mn₃O₄ thin film layer. According to reactions, additional washing may be performed with distilled water and/or an acid solution of 0.1 mM to 1 mM.

The organic solvent may include acetone, ethanol, tetrahydrofuran (THF), benzene, KOH/MeOH, MeOH, toluene, CH2C12, hexane, dimethylformamide (DMF), di-isopropyl ether, diethyl ether, dioxane, dimethylacetamide (DMA), dimethyl sulfoxide (DMSO), or chlorobenzene.

Specifically, the flocculated porous manganese oxide nanoparticles taken off while the binder is washed off the Mn₃O₄ thin film layer by the organic solvent are put aside, and the remaining alkaline metal or alkaline earth metal ions are washed out with distilled water. In some case, additional washing may be carried out with the acid solution, and water is injected for neutralization. The washed-off porous manganese oxide nanoparticles may be dispersed in water or organic solvent or may be dried into a powder.

Embodiment

Hereinafter, embodiments of the present disclosure are described in detail. However, the scope of the disclosure is not limited thereto.

Example of manufacturing a device for preparing porous manganese oxide nanoparticles

The Mn₃O₄ powder (commercially available from Avention, Inc., 0.94 g), Super-p (commercially available from MTI Korea, 0.03 g), and polyvinylidene fluoride (commercially available from Sigma-Aldrich, 0.03 g) were mixed together, and N-methyl-2-pyrrolidone (1 mL) (NMP, commercially available from Sigma-Aldrich) of 1 mL was added to the mixture, thus preparing slurry. The slurry was casted on a 25μm-thick copper sheet and was then dried in a vacuum oven, forming a 200 μm-thick Mn₃O₄ thin film layer. The formed Mn₃O₄ thin film layer was cut to a size of 8×8 cm². A 400μm-thick stainless steel (Sigma-Aldrich) sheet was cut to a size of 10×10 cm² and was used as an electrode. The electrode was placed on a case, with the copper sheet contacting the electrode, thereby forming an ion injector. A 20μm-thick, 12×12 cm²-sized polypropylene plate was placed on the Mn₃O₄ thin film layer of the ion injector. 1M of LiPF6 EC/DEC electrolyte was dropped on the polypropylene plate and then was wet, forming a separation plate. A 400μm-thick lithium sheet was cut to a size of 10×10 cm² and was placed on the electrode on the case, forming an ion generation layer. The separation plate was positioned between the Mn₃O₄ thin film layer and the lithium sheet, and the case was fastened up so that each layer inside comes in tight contact.

The reaction of the Mn₃O₄ thin film layer according to application of a voltage to the porous manganese oxide nanoparticles preparing device was measured and shown in FIG. 2.

An open circuit voltage in the so-manufactured porous manganese oxide nanoparticles preparing device was measured, and a resultant value of about 3V relative to lithium was obtained. Thereafter, as a constant current of −200μA is applied, the voltage gradually reduces from 3V and reaction thus occurs. If a reaction occurs, the curve turns flat at a specific reaction voltage. This indicates that a specific reaction continues to occur at the specific voltage, and the application of current continues until the reaction ends. The application of current may be regarded as the reaction occurring as, as many lithium ions as the number of electrons move.

Resultantly, between 1.2V and 0.8V, a conversion reaction is caused by the lithium ions and, as oxygen is taken off Mn₃O₄, the bonds increase in the early stage but, later, gradually decrease, so that atomization begins while Mn₃O₄ partially reduces into MnO₂. Then, at a lower voltage, an alloying reaction arises in which the lithium ions enter the Mn₃O₄ lattices, forming a new phase.

Embodiment: preparation of porous manganese oxide nanoparticles

−200 uA/cm² was applied to the porous manganese oxide nanoparticles preparing device, which was manufactured as above, to apply up to 0V (vs. Li+/Li). After the reaction ends, the porous manganese oxide nanoparticles preparing device was disassembled, and the Mn₃O₄ thin film layer was taken apart. The leftover electrolyte was washed off the Mn₃O₄ thin film layer using acetone. Next, the particles, taken off while the binder was washed off with the organic solvent, were put aside. Or, if not taken off by the organic solvent, the particles may be physically scrapped off and then put aside. Then, the taken-off particles were washed with 1 mM of acetone and then with water, thereby obtaining porous manganese oxide nanoparticles.

Comparative example: Mn₃O₄ particles

A Mn₃O₄ powder (commercially available from Avention Inc., 20 nm) as used in the preparation example was used in the comparative example.

EXPERIMENTAL EXAMPLE

Experimental Example: TEM Measurement

FIG. 3 illustrates the results of TEM measurement on the comparative example, FIG. 4 illustrates the results of high-resolution TEM measurement on the comparative example, and FIG. 5 illustrates the results of TEM measurement on an embodiment of the disclosure.

Referring to FIGS. 3 to 5, it may be identified that while the conventional Mn₃O₄ powder has a particle size of about 20 nm, the porous manganese oxide nanoparticles, according to an embodiment, includes about 5 nm primary nanoparticles. It is also identified that the Mn₃O₄ primary nanoparticles are partially reduced into MnO₂ primary nanoparticles. 

What is claimed is:
 1. Porous manganese oxide nanoparticles configured in a form of flocculated primary nanoparticles represented as in chemical formula 1 and primary nanoparticles represented as in chemical formula 2, wherein air pores are formed between the primary nanoparticles, wherein Mn₃O_(4-x)   [Chemical formula 1] wherein 0≤×≤0.4. MnO_(2-y)   [Chemical formula 2] wherein 0≤×≤0.2.
 2. The porous manganese oxide nanoparticles of claim 1, wherein a volume ratio of the primary nanoparticles represented as in chemical formula 1 to the primary nanoparticles represented as in chemical formula 2 ranges from 10% to 90%.
 3. The porous manganese oxide nanoparticles of claim 1, wherein the primary nanoparticles represented as in chemical formula 1 and the primary nanoparticles represented as in chemical formula 2 are uniformly mixed and flocculated.
 4. The porous manganese oxide nanoparticles of claim 1, wherein the primary nanoparticles represented as in chemical formula 1 or 2 have a size ranging from 0.3 nm to 6 nm.
 5. The porous manganese oxide nanoparticles of claim 1, wherein the porous manganese oxide nanoparticles have a porosity ranging from 10% to 40%.
 6. The porous manganese oxide nanoparticles of claim 1, wherein the air pores have a size ranging from 0.4 nm to 6 nm.
 7. The porous manganese oxide nanoparticles of claim 1, wherein the porous manganese oxide nanoparticles have a BET specific surface area ranging from 60 m²/g to 120 m²/g.
 8. Porous manganese oxide nanoparticles prepared by forming first nanoparticles represented as in chemical formula 1 in such a method as to separate Mn clusters by injecting positive ions into lattices of Mn₃O₄ particles and forming second nanoparticles represented as in chemical formula 2 by partially reducing the first nanoparticles, wherein Mn₃O_(4-x)   [Chemical formula 1] wherein 0≤×≤0.4. MnO₂   [Chemical formula 2] wherein 0≤×≤0.2.
 9. The porous manganese oxide nanoparticles of claim 8, wherein a volume ratio of the first nanoparticles represented as in chemical formula 1 to the second nanoparticles represented as in chemical formula 2 ranges from 10% to 90%.
 10. The porous manganese oxide nanoparticles of claim 8, wherein the first nanoparticles represented as in chemical formula 1 and the second nanoparticles represented as in chemical formula 2 are uniformly mixed and flocculated.
 11. The porous manganese oxide nanoparticles of claim 8, wherein the positive ions are positive ions of an alkaline metal or an alkaline earth metal.
 12. The porous manganese oxide nanoparticles of claim 8, wherein the positive ions are injected using a constant current or constant voltage method.
 13. A method for preparing porous manganese oxide nanoparticles, the method comprising: placing a Mn₃O₄ thin film layer and an ion generation layer on two opposite surfaces of a separation plate; and applying a voltage to the Mn₃O₄ thin film layer and the ion generation layer, wherein the ion generation layer includes an alkaline metal, an alkaline earth metal, an alkaline metal-containing alloy, or an alkaline earth metal-containing alloy.
 14. The method of claim 13, wherein the Mn3O₄ thin film layer is formed by casting slurry on a metal sheet and drying the slurry-cast metal sheet, the slurry formed by mixing an Mn₃O₄ powder, a binder, and an organic solvent.
 15. The method of claim 13, wherein the ion generation layer includes an alkaline metal, an alkaline earth metal, an alkaline metal-containing alloy, or an alkaline earth metal-containing alloy.
 16. The method of claim 13, wherein the separation plate is formed by wetting a porous polymer with an electrolyte. 